raremaprare-disease reference indexOrphadata 2026-06-23 · HPO 2026-09-01
ORPHA:2775

Autosomal recessive carpotarsal osteolysis

inactive · moved to ORPHA:371428Multicentric osteolysis-nodulosis-arthropathy spectrum

Synonyms: Hereditary multicentric osteolysis

Type
Disease
Group
Disorder
Status
inactive
Flag
Deprecated entity

This entity has been excluded from the Orphanet nomenclature of rare diseases and moved to Multicentric osteolysis-nodulosis-arthropathy spectrum

1

Names in Orphadata languages

12 of 12 languages
LangNameSynonyms
enAutosomal recessive carpotarsal osteolysisHereditary multicentric osteolysis
frOstéolyse carpotarsienne autosomique récessiveOstéolyse multicentrique
deOsteolyse, karpotarsale, autosomal-rezessiveOsteolyse, hereditäre multizentrische
esOsteólisis carpotarsiana autosómica recesivaOsteólisis multicéntrica hereditaria
itOsteolisi carpotarsale autosomica recessivaOsteolisi multicentrica ereditaria
nlAutosomaal recessieve carpotarsale osteolyseErfelijke multicentrische osteolyse
ptOsteólise carpo-társica autossómica recessivaOsteólise multicêntrica hereditária
plAutosomalna recesywna osteoliza nadgarstkowo-stępowaDziedziczna osteoliza wielocentryczna
csAutozomálně recesivní karpotarzální osteolýzaDědičná multicentrická osteolýza
ukАутосомно-рецесивний карпотарзальний остеолізСпадковий мультицентровий остеоліз
zh常染色体隐性腕跗骨骨质溶解遗传性多中心性骨质溶解
trOtozomal resesif karpotarsal osteolizKalıtsal çok merkezli osteoliz
2

Cross-references

qualifier = Orphanet mapping relation

No cross-references in this release.

3

Classification

Not placed in any Orphanet classification in this release.

No children.

4

Genes

0 direct

Orphanet records no gene directly on this code.

5

Prevalence and incidence

0 records

No prevalence record in this release.

6

HPO phenotypes

Orphanet has no HPO annotation for this code in this release.

7

Sources for this card